Canonical Allele Identifier: CA508043158
Gene: FUT2 HGNC NCBI

Linked Data

dbSNP Id: rs374665741
MyVariant Identifiers: chr19:g.49207155C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703898C>A , CM000681.2:g.48703898C>A GRCh38
NC_000019.9:g.49207155C>A , CM000681.1:g.49207155C>A GRCh37
NC_000019.8:g.53898967C>A NCBI36
NG_007511.1:g.12928C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.942C>A MANE Select ENSP00000387498.2:p.Ser314=
ENST00000522966.2:c.942C>A ENSP00000430227.2:p.Ser314=
ENST00000391876.5:c.942C>A ENSP00000375748.4:p.Ser314=
ENST00000425340.2:c.942C>A ENSP00000387498.2:p.Ser314=
NM_000511.5:c.942C>A NP_000502.4:p.Ser314=
NM_001097638.2:c.942C>A NP_001091107.1:p.Ser314=
NM_000511.6:c.942C>A MANE Select NP_000502.4:p.Ser314=
NM_001097638.3:c.942C>A NP_001091107.1:p.Ser314=
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